Canonical Allele Identifier: CA350827570

Gene: CUL3

Linked Data

• dbSNP Id: rs2106197314
• MyVariant Identifiers: chr2:g.225368487C>A (hg19) ; chr2:g.224503770C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503770C>A , CM000664.2:g.224503770C>A	GRCh38
NC_000002.11:g.225368487C>A , CM000664.1:g.225368487C>A	GRCh37
NC_000002.10:g.225076731C>A	NCBI36
NG_032169.1:g.86628G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1259G>T MANE Select	ENSP00000264414.4:p.Arg420Met
ENST00000264414.8:c.1259G>T	ENSP00000264414.4:p.Arg420Met
ENST00000344951.8:c.1061G>T	ENSP00000343601.4:p.Arg354Met
ENST00000409096.5:c.1187G>T	ENSP00000387200.1:p.Arg396Met
ENST00000409777.5:c.1187G>T	ENSP00000386525.1:p.Arg396Met
ENST00000481135.1:n.555G>T
ENST00000617432.4:c.-18G>T	ENSP00000477851.1:n.-18G>T
NM_001257197.1:c.1061G>T	NP_001244126.1:p.Arg354Met
NM_001257198.1:c.1277G>T	NP_001244127.1:p.Arg426Met
NM_003590.4:c.1259G>T	NP_003581.1:p.Arg420Met
XM_006712800.2:c.1226G>T	XP_006712863.2:p.Arg409Met
XM_011511994.1:c.1112G>T	XP_011510296.1:p.Arg371Met
XM_011511995.1:c.1217G>T	XP_011510297.1:p.Arg406Met
XM_011511996.1:c.1067G>T	XP_011510298.1:p.Arg356Met
XM_011511997.1:c.959G>T	XP_011510299.1:p.Arg320Met
XM_011511994.3:c.1112G>T	XP_011510296.1:p.Arg371Met
XM_011511996.2:c.1067G>T	XP_011510298.1:p.Arg356Met
NM_003590.5:c.1259G>T MANE Select	NP_003581.1:p.Arg420Met
NM_001257198.2:c.1277G>T	NP_001244127.1:p.Arg426Met
NM_001257197.2:c.1061G>T	NP_001244126.1:p.Arg354Met